Canonical Allele Identifier: CA1600466
Gene: SPAST HGNC NCBI

Linked Data

dbSNP Id: rs773913951
gnomAD v2: 2-32288949-A-C
gnomAD v4: 2-32063880-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32063880A>C , CM000664.2:g.32063880A>C GRCh38
NC_000002.11:g.32288949A>C , CM000664.1:g.32288949A>C GRCh37
NC_000002.10:g.32142453A>C NCBI36
NG_008730.1:g.5270A>C , LRG_714:g.5270A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.49A>C ENSP00000515816.1:p.Ser17Arg
ENST00000315285.9:c.49A>C MANE Select ENSP00000320885.3:p.Ser17Arg
ENST00000621856.2:c.49A>C ENSP00000482496.2:p.Ser17Arg
ENST00000642455.1:c.49A>C ENSP00000493827.1:p.Ser17Arg
ENST00000646571.1:c.49A>C ENSP00000495015.1:p.Ser17Arg
ENST00000315285.7:c.49A>C ENSP00000320885.3:p.Ser17Arg
ENST00000345662.5:c.49A>C ENSP00000340817.1:p.Ser17Arg
ENST00000615843.4:c.49A>C ENSP00000480893.1:p.Ser17Arg
NM_014946.3:c.49A>C , LRG_714t1:c.49A>C NP_055761.2:p.Ser17Arg
NM_199436.1:c.49A>C NP_955468.1:p.Ser17Arg
XM_005264516.3:c.49A>C XP_005264573.1:p.Ser17Arg
XM_011533067.1:c.49A>C XP_011531369.1:p.Ser17Arg
NM_001363823.1:c.49A>C NP_001350752.1:p.Ser17Arg
NM_001363875.1:c.49A>C NP_001350804.1:p.Ser17Arg
XM_005264516.5:c.49A>C XP_005264573.1:p.Ser17Arg
XM_011533067.2:c.49A>C XP_011531369.1:p.Ser17Arg
XM_017004778.2:c.49A>C XP_016860267.1:p.Ser17Arg
NM_001363823.2:c.49A>C NP_001350752.1:p.Ser17Arg
NM_001363875.2:c.49A>C NP_001350804.1:p.Ser17Arg
NM_001377959.1:c.49A>C NP_001364888.1:p.Ser17Arg
NM_014946.4:c.49A>C MANE Select NP_055761.2:p.Ser17Arg
NM_199436.2:c.49A>C NP_955468.1:p.Ser17Arg